Metal Oxygen Battery Containing Oxygen Storage Materials

ABSTRACT

In one embodiment, a metal oxygen battery system includes a metal oxygen battery having an electrode compartment. The electrode compartment includes an electrode being formed of an oxygen storage material. In another embodiment, the oxygen storage material includes an ion conducting component. In yet another embodiment, the oxygen storage material includes an electron conducting component. In yet another embodiment, the oxygen storage material includes a catalytic component. In yet another embodiment, at least one of the ion conducting component, the electron conducting component, and the catalytic component is attached to the oxygen storage material via a linker or as a pendant group.

BACKGROUND

1. Technical Field

One or more embodiments of the present invention relate to oxygenstorage materials as a source of oxygen for metal oxygen batteries andtheir method of use.

2. Background Art

There are many power storage and generation devices for vehicles. Forinstance, a fuel cell is a thermodynamically open system in which afuel, such as hydrogen, irreversibly reacts with an oxidant, such asoxygen, to form water and electrical energy. By contrast, a battery isan electrochemical device that is often formed of a number of separateelectrochemical battery cells interconnected to a single set ofterminals providing an electrical output.

SUMMARY

In one aspect of the present invention, a metal oxygen battery system isdisclosed. In one embodiment, the metal oxygen battery system includes abattery having an electrode compartment including an electrode beingformed of an oxygen storage material. In another embodiment, theelectrode compartment is sealed.

In yet another embodiment, the metal oxygen battery further includes asecond electrode compartment including a second electrode, the secondelectrode including a metal material (M), wherein the oxygen storagematerial is in communication with the second electrode. In yet anotherembodiment, the electrode and the second electrode are respectively acathode and an anode.

In yet another embodiment, the oxygen storage material has a pluralityof pores. In yet another embodiment, the pores contain an oxygenspecies. In yet another embodiment, the oxygen storage material includesan electron conducting component. In yet another embodiment, the oxygenstorage material includes an ion conducting component. In yet anotherembodiment, the oxygen storage material includes a catalyst component.

In yet another embodiment, the electrode has a first operating state ofoxygen physisorption into the oxygen storage material and a secondoperating state of oxygen release from the oxygen storage material. Inyet another embodiment, the electrode has a first operating state ofdeposition of an oxide of M into the oxygen storage material and asecond operating state of decomposition and release of at least aportion of the oxide of M from the oxygen storage material.

In yet another embodiment, the oxygen storage material has an oxygenvolumetric capacity greater than 2 grams of oxygen per liter of theoxygen storage material. In yet another embodiment, the oxygen storagematerial has an electron conductivity ranging from 1 Siemens percentimeter to 200 Siemens per centimeter at 25 degrees Celsius.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts an illustrative view of a battery system for use in avehicle according to one embodiment;

FIG. 2 illustrates a top view of an electric vehicle including a metaloxygen battery or a metal oxygen battery system according to anotherembodiment of the present invention;

FIG. 3 schematically illustrates in cross-sectional view a battery cellaccording to at least one embodiment;

FIGS. 4A to 4J schematically illustrate embodiments of crystallinestructures of metal organic frameworks; and

FIG. 5A to 5C schematically illustrate embodiments of themultifunctional electrode formed of oxygen storage material.

DETAILED DESCRIPTION

Reference will now be made in detail to embodiments of compositions,structures, and methods of the present invention known to the inventors.However, it should be understood that disclosed embodiments are merelyexemplary of the present invention which may be embodied in various andalternative forms. Therefore, specific details disclosed herein are notto be interpreted as limiting, rather merely as representative bases forteaching one skilled in the art to variously employ the presentinvention.

As required, detailed embodiments of the present invention are disclosedherein; however, it is to be understood that the disclosed embodimentsare merely exemplary of the invention that may be embodied in variousand alternative forms. The figures are not necessarily to scale; somefeatures may be exaggerated or minimized to show details of particularcomponents. Therefore, specific structural and functional detailsdisclosed herein are not to be interpreted as limiting, but merely as arepresentative basis for teaching one skilled in the art to variouslyemploy the present invention.

Except where expressly indicated, all numerical quantities in thisdescription indicating amounts of material or conditions of reactionand/or use are to be understood as modified by the word “about” indescribing the broadest scope of the present invention.

The description of a group or class of materials as suitable for a givenpurpose in connection with one or more embodiments of the presentinvention implies that mixtures of any two or more of the members of thegroup or class are suitable. Description of constituents in chemicalterms refers to the constituents at the time of addition to anycombination specified in the description, and does not necessarilypreclude chemical interactions among constituents of the mixture oncemixed. The first definition of an acronym or other abbreviation appliesto all subsequent uses herein of the same abbreviation and appliesmutatis mutandis to normal grammatical variations of the initiallydefined abbreviation. Unless expressly stated to the contrary,measurement of a property is determined by the same technique aspreviously or later referenced for the same property.

There are many power storage and generation devices for vehicles. Forinstance, a fuel cell is a thermodynamically open system in which afuel, such as hydrogen, irreversibly reacts with an oxidant, such asoxygen, to form water and electrical energy. By contrast, a battery isan electrochemical device that is often formed of a number of separateelectrochemical battery cells interconnected to a single set ofterminals providing an electrical output.

In one or more embodiments, the MOB 104 is substantially free of watermolecules and particularly liquid water molecules.

In one or more embodiments, the term “substantially free” refers to anextent of being less than 1000 parts per million (ppm), less than 500ppm, less than 200 ppm, less than 100 ppm, or less than 50 ppm. In someinstances means that a substance, such as water, is not purposefullyadded and whose presence, if any, is only incidental.

In yet another embodiment, the oxygen containment unit 102 includesrelatively pure oxygen species in that any other gas or fluid species,such as nitrogen (N₂), is not present or only incidentally present at anominal amount. This is in direct contrast to atmospheric air whereinnitrogen has a relatively significant presence relative to oxygen. Incertain instances, when incidentally present, nitrogen is less than 1000ppm, less than 500 ppm, less than 100 ppm, or less than 50 ppm.

As stated herein, one of the advantages of the present invention, in oneor more embodiments, is that oxygen can be stored in the oxygen storagematerial 110 with a relatively high concentration and/or density asunusable or interfering gas molecules such as nitrogen can beeffectively avoided. As a result, an oxygen material flow communicatingbetween the MOB 104 and the OSM 110 can be effectively in a relativelyhow flow rate, which further reduces system costs associated witheffecting and maintaining otherwise relatively high flow rateoperations.

Electrochemical battery cells can include numerous configurations andchemistries, including primary or non-rechargeable battery cells andsecondary or rechargeable battery cells. Non-limiting examples of asecondary battery cell include a lithium ion cell, a metal hydride cell,a metal-air battery cell, and a metal-oxygen battery cell. In general, asecondary battery cell is capable of storing electrical energychemically, and the chemical storage often involves a reversible redoxreaction. In the uncharged state, the redox reaction does not startspontaneously, and, in such cases, the secondary battery cell needs tobe charged initially in order to store energy.

In one example of a secondary battery cell, a lithium ion cell includesa layered oxide positive electrode including lithium in ioniccommunication with a graphite negative electrode through a non-aqueouselectrolyte and a separator. During charging, lithium is ionized fromthe layered oxide positive electrode and migrates through theelectrolyte and separator to the negative electrode and becomes embeddedin the porous negative electrode composition by the process ofintercalation. During a discharge half step, the intercalationcomposition decomposes allowing current to flow within the battery cellby the movement of lithium ions from the negative electrode to thepositive electrode.

In another example of a secondary battery cell, the metal hydridebattery cell includes a metal oxyhydroxide positive electrode, such as anickel oxyhydroxide, electrically communicating with a metal alloynegative electrode. The metal alloy negative electrode is a hydrogenstorage alloy negative electrode. The hydrogen storage alloy includes amaterial reversibly forming a mixture of metal hydride compounds. Incertain instances, the hydrogen storage alloy includes an intermetallicmaterial having two or more solid phase metallic elements.

In yet another example of a secondary battery cell, a metal air batterycell is, in typical configurations, an open system with respect tomaterial flow, heat transfer, and work. For instance, a metal airbattery cell is provided with holes, openings, or vents, which mediateair transport between the metal air battery and atmospheric air. Formost metal air batteries, moisture and interfering gases from the airoften need to be filtered, eliminated, or trapped prior to the air'sbeing introduced to the metal air battery. For instance, the metal airbattery cell includes an air positive electrode electricallycommunicating with a metal negative electrode through an electrolyte anda separator. The air positive electrode, in typical configurations,includes a carbon composition positive electrode. During the chargereaction, oxygen is released to the ambient air.

Metal oxygen batteries (MOBs) are conventionally characterized as asubgroup of the metal air batteries as oxygen is commonly involved forthe electrochemical reactions. MOBs are known to have relatively highelectrochemical capacities, and are therefore of great interest forapplications where the total mass of a given battery is limited.Implementation of conventional MOBs has been met with difficulties inthat their performance, both in terms of capacity and power, has beenlargely unsatisfactory. The limited performance is believed to be atleast in part associated with incomplete or slow reactions involving thearrival and diffusion of oxygen molecules. For an MOB to achieve itsfull discharge capacity, sufficient quantities of oxygen must be madeavailable in a timely manner. In addition, since the rate of dischargingis tied to the formation and growth of the positive electrode oxide, thebattery's rate of discharging at least in part depends on the more ratelimiting processes of oxygen diffusion.

In one or more embodiments, the term metal oxygen battery (MOB) refersto a battery structure that differs from conventional metal oxygen/airbatteries at least in that the MOB is relatively closed to atmosphericair and oxygen for reactions is relatively devoid of unwanted speciessuch as nitrogen or carbon dioxide.

In one or more embodiments, the term “electrode” may refer to astructure through which charges are carried by electromotive force.Electrodes may be composed of one or more metal and/or semiconductor.Electrodes may be solid or liquid.

In one or more embodiments, the term “electrolyte” refers to a materialand/or structure through which charges are carried by the movement ofions. Electrolytes may be any phase on the continuum of liquid to solid,including polymer gels, pastes, fused salts, ionic liquids, organiccarbonates, or ionically conducting solids, such as sodium β-alumina,which has mobile sodium ions.

In one or more embodiments, metal-oxygen batteries (MOBs) may refer to aclass of electrochemical cells in which, during discharging, oxygen isreduced at a positive electrode surface as part of the electrochemicalcell reaction. Reduction of the oxygen forms an oxide or peroxide ionwhich reacts with a cationic metal species. Metal-oxygen batteries maybe based upon Fe, Zn, Al, Mg, Ca, and Li.

MOBs, such as Li⁺ based MOBs, have recently been demonstratedexperimentally in a small number of laboratories. However,implementation of conventional MOBs has been largely unsuccessfulbecause their performance, both in terms of capacity and power, has beenunsatisfactory for vehicle applications. The limited performance isbelieved to be likely associated with incomplete or slow reactionsinvolving the arrival and dissociation of oxygen molecules from theatmospheric air. In particular, for a metal oxygen battery to achieveits full discharge capacity, sufficient quantities of oxygen should bemade available in a timely manner. In addition, since the rate ofdischarge is tied to the formation and growth of the cathode oxide, thebattery's rate of discharge depends in part on the more rate limitingprocesses of oxygen dissociation.

It has been found, according to one or more embodiments of the presentinvention, that the MOB performance can be greatly improved by one ormore of the following approaches: (1) providing a relatively highconcentration of oxygen at the positive electrode; and/or (2) increasingoxygen diffusion rate at the positive electrode.

One or more of the following benefits can be realized according tocertain embodiments of the present invention: (1) requirements for manybalance of plant (BOP) components including positive electrode flowfield, blower, and air purification system, can be reduced oreliminated; (2) susceptibility to contamination from atmospheric airimpurities can be reduced or eliminated; (3) battery system flexibilitymay be increased and packaging costs can be reduced ; (4) battery cellmanufacturing procedures may be simplified; and/or (5) improved batteryperformance kinetics may be realized via a reduction in bulk diffusionand an increase in surface diffusion.

According to one aspect of the present invention, a battery system isprovided. In one embodiment, and as depicted in FIG. 1, a battery systemgenerally shown at 100 includes a metal oxygen battery 104 having afirst electrode 104 a and a second electrode 104 b, the second electrode104 b including a metal material M (not shown). An oxygen storagematerial 110 is disposed within the metal oxygen battery 104. In certaininstances, the metal oxygen battery 104 further includes a separator 116defining a first electrode compartment 112 including the first electrode104 a and a second electrode compartment 114 including the secondelectrode 104 b. In this configuration, the oxygen storage material 110is disposed within the first electrode compartment 112 and communicatesoxygen 108 to and from the first electrode 104 a.

In certain instances, the oxygen storage material 110 is in fluidcommunication with the metal oxygen battery 104, and in certainparticular instances the fluid is oxygen.

In one or more embodiments, the metal material M includes one or moreelemental metal listed in the periodic table and/or one or more alloysformed of a mixture of two or more of the elemental metals. Anon-limiting list of the elemental metals includes alkali metals,alkaline earth metals, transition metals and post-transition metals. Incertain instances such as during discharging, the first electrode 104 afunctions as a positive electrode or a cathode, and the second electrode104 b functions as a negative electrode or an anode. In certain otherinstances such as during charging, the first electrode 104 a mayfunction as a negative electrode or an anode, and the second electrode104 b may function as a positive electrode or a cathode. In theseinstances, the term “positive electrode” refers to an electrode with apositive polarity, and the term “negative electrode” refers to anelectrode with a negative polarity.

FIG. 2 illustrates a top view of an electric vehicle including a metaloxygen battery or a metal oxygen battery system according to anotherembodiment of the present invention. As illustratively depicted in FIG.2, connected to vehicle 218 is a metal oxygen battery (MOB) system 220electrically communicating directly or indirectly with a controller 230.The controller 130 electrically communicates with a traction motor 226.Traction motor 226 is connected to at least one wheel 228 of the vehicle218. In certain instances, MOB battery system 220 electricallycommunicates with and provides energy to a high-voltage bus 222.High-voltage bus 222 electrically communicates with and provides energyto a power conditioner 224. The power conditioner 224 electricallycommunicates with the traction motor 226 which is connected directly orindirectly to wheel 228 situated on a frame 232.

Turning now to FIG. 3, a battery cell 330 is schematically illustratedin cross-sectional view according to at least one embodiment. A firstelectrode 332 electrically communicates with a second electrode 334. Thefirst electrode 332 and second electrode 334 are situated in a housing336. Housing 336 defines a closed container allowing no transfer ofmaterial, oxygen in particular, to and from the ambient environment, butallows heat and work to be transferred.

A separator 338 may be situated between the first electrode 332 and thesecond electrode 334. In this configuration, the first electrode 332,the second electrode 334, and the separator 338 are contained within thehousing 336 and are at least partially in contact with an electrolyte340. In certain particular instances, the electrolyte 340 isnon-aqueous.

Conduit 342 extends from housing 336 and electrically communicates withfirst electrode 332. Conduit 344 also extends from housing 336 andelectrically communicates with electrode 334. Conduits 342 and 344electrically communicate with high voltage bus 222 to allow electrons toflow between the first electrode 332 and second electrode 334 when thecircuit 314 is in a closed operating state.

In yet another embodiment, an enlarged view 504, 506, 508, 510 of asection 502 of the first electrode 104 a is depicted in FIGS. 5A to 5C.As illustrated by the enlarged view 504, at least a portion of the firstelectrode 104 a may be formed of OSM that has all the followingfunctions: particular porosity for oxygen storage, particular catalyticcapacity, particular ion conductivity, and particular electronconductivity. As illustrated by the enlarged view 506, at least aportion of the first electrode 104 a may be formed of OSM deficient ofone or more of the above-categorized functions, and supplemented, forinstance, with an ion conductive material 512. As illustrated by theenlarged view 508, at least a portion of the first electrode 104 a maybe formed of OSM deficient of one or more of the above-categorizedfunctions, and supplemented, for instance, with an electron conductivematerial 514. As illustrated by the enlarged view 510, at least aportion of the first electrode 104 a may be formed of OSM deficient ofone or more of the above-categorized functions, and supplemented, forinstance, with a catalytic material 516.

An operating state, in at least one embodiment, includes a dischargingoperating state, in which oxidation occurs at the second electrodeproducing electrons. A non-limiting example of a half-cell reaction atthe second electrode during discharging operating state is shown in [1]

Li→Li⁺+e⁻  [1]

where the Li metal is included in the second electrode and the Li cationmigrates through the electrolyte to the first electrode. At the firstelectrode, the Li cation reacts with oxygen to form the mixed oxidemetal oxide as shown in [2]

Li⁺+xO₂+2×e⁻→LiOx   [2]

where the electrons generated at the second electrode in [1] flow to thefirst electrode through a load circuit, such as high voltage bus 14; andwhere LiOx may be the mixed oxide metal oxide which may includestoichiometric metal oxides such as Li₂O₂, a lithium peroxide and Li₂O,a lithium oxide. It is appreciated that non-stoichiometric metal oxidesmay be intermixed with the stoichiometric metal oxides or comprise theentire mixed oxide metal oxide, especially after at least greater than10 charging-discharging cycles have occurred. A non-limiting example ofthe non-stoichiometric metal oxide may include a dendritic mixed oxidemetal oxide solid that forms at the second electrode. While not wishingto be tied to any one theory, the formation of such irregular mixedoxide metal oxide solids, such as the dendritic mixed oxide metal oxidemay be one cause of the long-term degradation of the effectiveness ofbeing able to recharge the MOB.

Without being limited to any particular theory, it is believed thatoxygen storage material as disposed within a metal oxygen battery doesnot lose surface area or deactivate to any significant degrees, underthe normal operating conditions for the metal oxygen battery. In certaininstances, at least 70 percent, 80 percent, 90 percent, or 98 percent byweight of the oxygen storage material remain thermally stable andelectrochemically active after 3 months of usage.

At the second electrode during the charging operating state, followingthe above embodiment and non-limiting example, reduction occurs as thelithium cation is reduced to lithium metal at the second electrode. Theexemplary half-cell reaction is shown in [3]

Li⁻+e⁻→Li   [3]

At the first electrode during the charging operating state, oxidationoccurs, producing electrons and decomposing the mixed oxide metal oxidesolid to release oxygen. A non-limiting example of a half-cell reactionat the first electrode during the charging operating state is shown in[4]

$\begin{matrix}{{{LiO}x}->{{Li}^{+} + {\frac{x}{2}O_{2}} + e^{-}}} & \lbrack 4\rbrack\end{matrix}$

The oxygen is stored in an oxygen containment unit including the OSMwhen the oxygen is contained by physiosorption intercalation, and/orclathratization. The OSM may be situated in an external storage device,permitting isolation of the OSM from the first electrode; adjacent tothe first electrode; and/or in intimate contact with the firstelectrode, which substantially minimizes the diffusion distance for theoxygen until reaction with the first electrode occurs during thedischarging operating state. Reducing the diffusion distance increasesthe responsiveness to electron flow rates as the demand on the loadcircuit, e.g. directly or indirectly the demand of the traction motor,changes during operation time periods of the vehicle.

In at least one embodiment, the average diffusion distance from thepoint of the OSM where oxygen is released to the point at or near thefirst electrode where the oxygen is reacted to is from 1 nm to 5 cm, 1nm to 1 cm, or 1 nm, to 0.1 cm.

In one or more embodiments, the metal-oxygen battery cell is aclosed-loop system with respect to material flow, but not to heattransfer or work. For instance, the metal-oxygen battery cell includesan oxygen positive electrode electrically communicating with a metalnegative electrode through an electrolyte and a separator. The oxygenpositive electrode includes an oxygen storage material which storesoxygen by the process of physiosorption, including adsorption,intercalation and clathratization processes. It should be appreciatedthat the oxygen positive electrode may further include a structuralcomponent in addition to the oxygen storage material, such as a carbonmaterial. It is appreciated that the metal-oxygen battery positiveelectrode may further include a catalytic component, such as Fe₂O₃and/or Co₃O₄; an ion conductive component, such as polyacrylonitrileand/or polyethylene oxide; and/or an electron conductive componentincluding a conductive aid, such as amorphous carbon, graphitic carbon,graphene, and/or carbon nanotubes.

In one or more embodiments, the metal-oxygen battery cell undergoesreversible redox reactions. During the discharging reaction, the oxygenreacts with a metal cation from the metal negative electrode, forming amixed oxide metal oxide, including a metal oxide and/or a metal peroxidewhich is then situated at the positive electrode. During the chargingreaction, the metal mixed oxide metal oxide decomposes, releasing oxygenwhich, in at least one embodiment, is stored in a metal oxygen framework(MOF) composition at the positive electrode. The metal cation migratesback to the negative electrode reacquiring an electron from the negativeelectrode and forming a metal composition.

Oxygen storage materials (OSMs) may be utilized for oxygen by providingappreciable surface area for enhancing oxygen uptake. Desirable on-boardoperating conditions illustratively include near ambient temperature (T)(e.g., 150 K to 400 K) and modest pressure (P) (e.g., 1 to 100 bar) toavoid added cost or system complexity. Particularly suitable bindingenergies for oxygen material storage may be determined based on theClausius-Claeypron Equation of the form:

${\ln \; P} = {\frac{{- \Delta}\; H}{R}\frac{1}{T}}$

where P is the partial pressure of oxygen, ΔH is the sorbent oxygenbinding energy, R is a constant, and T is the temperature in degreesKelvin of the oxygen. In certain other instances, the OSM has an oxygenbinding energy, or particularly an isosteric adsorption enthalpy,ranging from 5 kJ/mol.O₂ to 100 kJ/mol.O₂, or 7 kJ/mol.O₂ to 70kJ/mol.O₂, or to 10 kJ/mol.O₂ to 40 kJ/mol.O₂.

In one or more embodiments, OSMs may be utilized as oxygen storagematerials for oxygen in terms of having relatively high materialdensity. The volumetric storage capacity of an OSM may be related to thegravimetric capacity and material density for the OSM. As a non-limitingexample, if a given OSM has a gravimetric capacity of 0.3 kg of oxygenper kg and a materials density of 0.2 g/mL, a corresponding volumetriccapacity would be 60 g of oxygen per liter of OSM. Storing 8 kg ofoxygen would use 133 liters of OSM. However, if the material density is1 g/mL, only 27 liters of OSM would be required.

Without being limited to any particular theory, it is appreciated thatthe OSMs are generally provided with a relatively high-surface area,which facilitates oxygen uptake or adsorption by processes such asphysiosorption. Such oxygen uptake scales linearly with surface area asmeasured using any suitable method such as the BET method. In certaininstances, the surface area of the OSM exceeds 1000 m²/g, from 2000 m²/gto 8000 m²/g, or from 3000 m²/g to 6000 m²/g.

In one or more embodiments, it is appreciated that oxygen molecules asdescribed herein may include oxygen species other than oxygen, such asdiatomic oxygen, ozone, and free radical oxygen species.

In certain instances, the OSM in the excess capacity has a gravimetriccapacity for oxygen of greater than 10 grams per 100 grams of the OSM,or of between 20 to 80 grams per 100 grams of the OSM, or 25 to 50 gramsoxygen per 100 grams of the OSM.

In certain other instances, the OSM has a material (single crystal)density greater than 0.1 g/mL, or of from 0.25 g/mL to 5 g/mL, or offrom 0.5 g/mL to 2 g/mL.

In certain other instances, the OSM has a volumetric capacity for oxygenof greater than 2 g/L, or of from 16 g/L to 500 g/L, of or 32 g/L of to300 g/L, or of from 50 g/L to 220 g/L.

In one or more embodiments to achieve one or more of the propertiesdiscussed above, the OSMs are porous, high surface area sorbentmaterials. Non-limiting examples of the OSMs include crystallineframework-like compounds such as metal-organic frameworks (MOFs),covalent organic frameworks (COFs), zeolitic imidazolate frameworks(ZIFs) and zeolitic materials; aerogel-like substances with nanometer ormicrometer scale porosity, such as zero-gels and xero-gels; porouscarbon materials such as porous carbon gels, porous carbon nanotubes,and porous metal substances such as porous metal oxides, porous metalcarbides, porous metal nitride or other porous metal substances withinternal sites that favorably form weak physical adsorption sites withoxygen.

Non-limiting examples of the MOFs include: a catalytically-active MOF-5having embedded metal, such as Ag@ [Zn₄O(BDC)₃], Pt@ [Zn₄O (BDC) ₃], Cu@[Zn₄O (BDC) ₃], and Pd@ [Zn₄O(BDC)₃]; an organically solvated MOF, suchas Ti(O^(i)Pr)₄[Cd₃Cl₆(LI)₃.4DMF.6MeOH.3H₂O,Ti(O^(i)Pr)₄[Cd₃(NO₃)₆(LI)₄.7MeOH.5H₂O, Ti(O^(i)Pr)₄[Cd(LI)₂(H₂O)₂][ClO₄]₂.DMF.4MeOH.3H₂O, [Rh₂(M²⁺TCPP)₂], where M²⁺ may include Cu, Ni,or Pd, and [Zn₂(BPDC)₂(L2)].10DMF.8H₂O; an ionically or partiallyionically solvated MOF, such as [Ni(L-aspartate)bpy_(0.5)]HCl_(0.9)MeOH_(0.5),[Cu(L-aspartate)bpy_(0.5)]HCl, [Cu(D-aspartate)bpy_(0.5)]HCl,[Cu(L-aspartate)bpy_(0.5)]HCl, [Cu(D-aspartate)bpy_(0.5)]HCl, Cr₃(F, OH)(en)₂O(BDC)₃(ED-MIL-101), Cr₃(F, OH)(en)₂O(BDC)₃(ED-MIL-101), [Zn₃O(L3-H)].(H₃O)₂(H₂O)₁₂(D-POST-1), [Sm(L4-H₂)(L4-H₃)(H₂O)₄].(H₂O)_(x),[Cu(bpy)(H₂O)₂(BF₄)(bPY)], [Zn₄O(BDC)₃](MOF-5),[Ln(OH)H₂O)(naphthalenedisulfonate)] where Ln includes a lanthanidemetal such as Nd, Pr, or La; as well as [In₄(OH)₆(BDC)₃], [Cu₃(BTC)₂],[Sc₂(BDC)₃], [Sc₂(BDC)_(2.5)(OH)], [Y₂(BDC)₃(H₂O)₂].H₂O,[La₂(BDC)₃(H₂O)₂].H₂), [Pd(2-pymo)₂], [Rh₂(H2TCPP)₂) BF₄, [Cu₂(trans-1,4cyclohexanedicarboxylate)₂]H₂O, [Cu(2-pymo)₂], [Co(PhIM)₂],[In₂(BDC)₃(bPY)₂], [In₂(BDC)₂(OH)₂(phen)₂], [In(BTC)(H₂O)(bpy)],[In(BTC)(H₂O)(phen)], [Sc₂(BDC)_(2.5)(OH)], [Y₂(BDC)₃(H₂O)₂].H₂O,[La₂(BDC)₃(H₂O)₂]H₂O, [Cu₃(BTC)₂], [Cd(4,4′-bPy)₂(H₂O)₂]—(NO₃)₂.(H₂O)₄,[Sm(L4-H₂)(L4-H₃)(H₂O)₄].(H₂O)_(x), Mn₃[(Mn₄Cl)(BTT)₈(MeOH)₁₃]₂,[Zn₄O(BDC)₃](MOF-5), Ti-(2,7-dihydroxynaphthalene)-MOF, [Pd(2-pymo)₂],[Cu₃(BTC)₂], [Cu₃(BTC)₂], [Cu₃(BTC)₂], [Rh₂(L5)],[Rh(BDC)],[Rh(fumarate)], [Ru(1,4-diisocyanobenzene)₂]Cl₂, [In₄(OH)₆(BDC)₃],[Ru₂(BDC)₂], [Ru₂(BPDC)₂], [Ru₂(BDC)₂(dabco)], [Ru₂(BPDC)₂(dabco)],[Rh₂(fumarate)₂], [Rh₂(BDC)₂], [Rh₂(H₂TCPP)₂], and [Pd(2-pymo)₂].

In certain instances, the MOF has a general composition of M@MOFgas-phase deposited nanoparticles, such as Pt@ [Zn₄O (BDC)₃]. The M′@MOFgas-phase deposited nanoparticles may have an average maximum dimensionranging from 0.5 nm to 5 nm, or 0.75 nm to 3.5 nm, when fresh. In atleast one embodiment, M′ includes one or more polynuclear metal clustersand/or any metal-containing molecule such as Fe₂O₃, Co₃O₄, or mixturesof metal-containing molecules. Therefore, M′ can additionally serve asone or more catalytic components for catalyzing the reactions within themetal oxygen battery.

In at least one embodiment, the M′ content of the M′@MOF material rangesfrom 5 percent to 35 percent by weight, or 20 percent to 30 percent byweight, of the M′@MOF material.

In at least one embodiment, the electron conductive component includes apost-synthesized substituent, such as a pendant chain having an electronconductive functional group, such as an acrylonitrile group or acyano-group. In another embodiment, the electron conductive componentincludes a conductive polymeric molecule, having the electron functionalgroup in the polymeric chain prior to binding with the metal atomforming the MOF. In certain instances, one or more of these electronconductive components may be coupled to the MOF molecules as linker or apendant groups to confer electron conductive functions to the MOF-basedelectrode.

In certain particular instances, the electron conductive component has aconductivity ranging from 1 Siemens/cm to 200 Siemens/cm, 10 Siemens/cmto 150 Siemens/cm, 20 Siemens/cm to 100 Siemens/cm, 30 Siemens/cm to 60Siemens/cm.

Ion conducting components assist in ion transport within one MOF crystaland between MOF crystals. Ions in MOF may provide a capacitive functionin the battery system in order to provide relatively rapid chargerelease. Non-limiting examples of the ion conductive components includea carbon nanoparticle, such as a single-wall carbon nanotube, amulti-wall carbon nanotube, a Y-shaped carbon nanotube, a carbonnanoribbon, and/or a carbon microfiber. In certain instances, the ionconductive component includes a carbon structure, such as a graphenesheet. In certain other instances, the ion conductive component is anion-exchanged ion conductive component.

Referring now to FIG. 4A, an MOF crystal is schematically illustrated.As depicted in FIG. 4A, an MOF of the structure M′@MOF having agas-phase deposited metal (M′) generally shown at 400 includes a metalatom with carboxylate oxygen 402 which is connected to a bridging ligand404. Metal atom and bridging ligand 404 collectively define a cavity 406into which gas-phase deposited metal 408 (M′) and oxygen molecule 410are situated. In at least one embodiment, the MOF 400 is anisorecticular MOF wherein all 12 bridging ligands 404 are identical toeach other.

In another embodiment, as illustrated in FIG. 4B, an MOF with anelectron conductive component 420 is schematically illustrated. Metalatom with carboxylate oxygen 402 is bridged by a first bridging ligand404 a and/or a second bridging ligand 404 b. In certain instances, thesecond bridging ligand 404 b is longer than the first bridging ligand404 a. The resulting MOF is heterorecticular. The metal atom 402 andbridging ligands 404 a, 404 b collectively define a cavity 406. Pendantfrom the second bridging ligand 404 b is an electron conductivecomponent 420. Non-limiting examples of a conductive component 420include a polyacrylonitrile substituent and/or a cyano-substituent. Itis appreciated that electronic conductive component 420 can be bonded toeither first bridging ligand 404 a and/or second bridging ligand 404 b.Further, it is appreciated that not all bridging ligands need to have anelectron conductive component. The electronically conductive groups 404a and 404 b do not have to be pendent, in that they can be linkergroups. It is yet further appreciated that electron conductive component420 may be a different chemical species for one or more bridging ligandwithout exceeding the scope or spirit of the embodiment. Furtherincluded in MOF 400 is an oxygen molecule 410, which is optional, andmay be present or absent depending upon the operating state in which theMOF is situated.

In yet another embodiment, as schematically illustrated in FIG. 4C, anMOF 400 with a guest molecule 444 is illustrated. MOF 400 includes metalatom 402 with bridging ligand 404 a and 404 b. The metal atom 402 andthe ligands 404 a, 404 b collectively define a cavity 406. Situatedinside the cavity 406 is one or more oxygen molecules 410 and one ormore guest molecules 444. Non-limiting examples of the guest molecule444 include solvents, solvents used to prepare the OSM, or electrolytesolvents. Non-limiting examples of the solvents for OSM synthesisinclude ethanol, dimethylformamide, diethylformamide, andtetrahydrofuran. It is appreciated that that while FIG. 4C shows onlyone or two guest molecules 444, in another embodiment a plurality oftypes of guest molecules could be contemplated without exceeding thescope or spirit of the embodiment.

In yet another embodiment, as illustrated in FIG. 4D, an MOF generallyshown at 400 includes deposited metal M′408, an electron conductivecomponent 420, and an ion conductive component 462 such as an organiccarbonate. Metal atom 402 and the bridging ligands 404 a, 404 bcollectively define a cavity 406. Received within the cavity 406 may beone or more electron conductive components 420, one or more ionconductive components 462, and/or one or more oxygen molecules 410.

In yet another embodiment, as illustrated in FIG. 4E, an MOF 400 havingone or more electron conductive components 420 and/or one or more guestmolecules 444 is schematically illustrated. In this arrangement, metalatom with carboxylate oxygen 402 and bridging ligand 404 collectivelydefine a cavity 406, into which one or more oxygen molecules 410 arereceived.

In another embodiment, as schematically illustrated in FIG. 4F, an MOF400 is schematically illustrated. Metal atom 402 and bridging ligand 404define a cavity 406. Received within the cavity 406 can be one or moregas-phase deposited metals M′408, one or more electron conductivecomponents 420, and/or one or more oxygen molecules 410.

In yet another embodiment, as shown in FIG. 4G, an MOF 400 includesmetal atoms 402 and bridging ligands 404, collectively defining a cavity406. Received within the cavity 406 may be one or more gas-phaseddeposited metal M′408, one or more ion conductive components 420, and/orone or more oxygen molecules 410. In certain instances, the MOF 400 maybe disposed next to a graphite sheet 424 to be provided with additionalelectron conductivity.

In yet another embodiment, as shown in FIG. 4H, an MOF 400 isschematically illustrated. The MOF 400 includes metal atoms 402 bridgedwith a first bridging ligand 404 and a second bridging ligand 446. Thesecond bridging ligand 446 is cyano-substituted. Cyano-substitutedbridging ligand 446 is electronically conductive and different in chainlength from the first bridging ligand 404. This MOF is thus aheterorecticular MOF crystal. The metal atoms 402, the first bridgingligand 404 and the second cyano-substituted bridging ligand 446collectively define a cavity 406. One or more oxygen molecules 410 canbe received within the cavity 406.

In another embodiment, as schematically illustrated in FIG. 4I, an MOF400 includes metal atom 402 and multidentate ligand 446, which connectsa plurality of metal atoms 402. The ligands 446 and the metal atoms 402collectively define a cavity 406. Received within the cavity 406 may beone or more gas-phase deposited metals M₁ 408 and oxygen molecules 410.

In another embodiment, as illustrated in FIG. 4J, an interpenetratingnetwork of two MOFs 400 a and 400 b is generally illustrated at 400. InMOF 400 a, metal atoms 402 and bridging ligands 404 define cavity 406into which MOF 400 b partially interpenetrates. The result is that MOFcavity 406 has a reduced volume for accepting oxygen molecules thanwould be otherwise expected based on the chain length of bridging ligand404. Having interpenetrating MOFs may result in certain reduction of theabsolute pore capacity, but the pore capacity and transfer of gasmolecules between MOF crystals may be controlled by havinginterpenetrating MOFs.

In one or more embodiments, the MOF is a porous coordination network(PCN) having at least one entactic metal center (EMC), such as PCN-9MOF. The EMC is an unusual geometry imposed by a ligand on a metalcenter in the MOF for the purpose of enhancing the MOF's affinity foroxygen. Non-limiting examples of imposed geometry include adaptingorganic positive electrode units to generate a pore comparable to thesize of the oxygen molecule and introducing a coordinatively unsaturatedmetal center, such as a metal cation cluster. A combination of severalEMCs may create a secondary building unit (SBU) within the MOF suitablefor exceptional gas sorption affinity as determined by adsorptionisotherms collected at various temperatures and fitted using theLangmuir-Fruendlich equation.

When applied as an example of the OSM, and in certain instances, PCN-9may be provided with an oxygen adsorption enthalpy greater than 12kJ/mol.O₂, ranging from 15 kJ/mol.O₂ to 45 kJ/mol.O₂, from 17 kJ/mol.O₂to 43 kJ/mol.O₂, or 18 kJ/mol.O₂ to 23 kJ/mol.O₂. PCN-9 has a fixed porediameter ranging from 0.55 nm to 0.75 nm or 0.6 nm to 0.7 nm.

In certain instances, the MOF includes a solvated MOF formed from1,4-benzenedicarboxylic acid (BDC) with a zinc metal cation cluster. Anon-limiting example of the solvated MOF is Zn₄ (μ-4 O) (j-BDC)₃.DEF)₇,where DEF is diethylformamide, a solvent molecule.

An example of a manufacturing process for certain MOFs, such as theMOF-5, includes the steps of mixing a solution of terephthalic acid witha zinc salt, such as zinc nitrate to form a mixture. The mixture iscrystallized or precipitated at a temperature ranging from 25° C. to200° C. The precipitate is filtered from the solution and dried. It isappreciated that MOFs may be modified after synthesis via reactions suchas oxidation, acetylization, hydrogenation, Knoevenagel condensation,and/or Heck coupling. Moreover, the MOFs may be activated by removingthe solvent introduced during a crystallization and/or precipitationprocess.

In one or more embodiments, the second electrode 104 b , which functionsas an anode during discharging, includes a metal material (M). The metalmaterial M may include a metal, such as an alkali metal, analkaline-earth metal, or a transition metal. The metal material M mayalso include alloys of such metals, metal ceramics, superalloys, fusiblealloys, metal intercalation compounds or materials, and amalgams. Incertain particular instances, the metal material M includes an elementalmonolith negative electrode, including, for example, Li or Na; a mixedmaterial negative electrode, having an intercalation compound, such asgraphite; and/or an alloy, such as a lithium-silicon alloy, a lithiumaluminum alloy, and/or a lithium boron alloy.

In certain particular instances, the second electrode 104 b is formed ofelemental lithium metal. In certain other particular instances, thesecond electrode 104b includes an alloy of lithium.

The following applications disclose and claim battery systems that maybe related to the battery system disclosed and claimed herein: U.S.patent application Ser. Nos: ______, ______, _____, _____, and ______,all filed on ______. Each of the identified applications is incorporatedherein by reference in their entirety.

While the best mode for carrying out the invention has been described indetail, those familiar with the art to which this invention relates willrecognize various alternative designs and embodiments for practicing theinvention as defined by the following claims.

1. A metal oxygen battery system comprising: a metal oxygen batteryhaving an electrode compartment including an electrode being formed ofan oxygen storage material.
 2. The metal oxygen battery system of claim1, wherein the electrode compartment is sealed.
 3. The metal oxygenbattery system of claim 1, further comprising a second electrodecompartment including a second electrode, the second electrode includinga metal material (M), wherein the oxygen storage material is incommunication with the second electrode.
 4. The metal oxygen batterysystem of claim 3, wherein the electrode and the second electrode arerespectively a cathode and an anode.
 5. The metal oxygen battery systemof claim 1, wherein the oxygen storage material has a plurality ofpores.
 6. The metal oxygen battery system of claim 5, wherein the porescontain an oxygen species.
 7. The metal oxygen battery system of claim1, wherein the oxygen storage material includes an electron conductingcomponent.
 8. The metal oxygen battery system of claim 1, wherein theoxygen storage material includes an ion conducting component.
 9. Themetal oxygen battery system of claim 1, wherein the oxygen storagematerial includes a catalyst component.
 10. The metal oxygen batterysystem of claim 1, wherein the oxygen storage material includes acatalyst component and an electron conducting component.
 11. The metaloxygen battery system of claim 1, wherein the oxygen storage materialincludes a catalyst component and an ion conducting component.
 12. Themetal oxygen battery of claim 1, wherein the oxygen storage materialincludes an ion conducting component and an electron conductingcomponent.
 13. The metal oxygen battery of claim 1, wherein the oxygenstorage material includes a catalyst component, an ion conductingcomponent and an electron conducting component.
 14. The metal oxygenbattery of claim 1, wherein the electrode has a first operating state ofoxygen physisorption into the oxygen storage material and a secondoperating state of oxygen release from the oxygen storage material. 15.The metal oxygen battery system of claim 1, wherein the electrode has afirst operating state of deposition of an oxide of M into the oxygenstorage material and a second operating state of decomposition andrelease of at least a portion of the oxide of M from the oxygen storagematerial.
 16. The metal oxygen battery system of claim 1, wherein theoxygen storage material has an oxygen volumetric capacity greater than 2grams of oxygen per liter of the oxygen storage material.
 17. The metaloxygen battery system of claim 1, wherein the oxygen storage materialhas an electron conductivity ranging from 1 Siemens per centimeter to200 Siemens per centimeter at 25 degrees Celsius.
 18. The metal oxygenbattery system of claim 1, wherein the oxygen storage material includesa material selected from the group consisting of metal-organicframeworks (MOFs), covalent organic frameworks (COFs), zeoliticimidazolate frameworks (ZIFs), and combinations thereof.
 19. A metaloxygen battery comprising: a first electrode compartment including afirst electrode and a second electrode compartment including a secondelectrode, the first electrode being formed of an oxygen storagematerial, the second electrode including a metal material (M), theoxygen storage material being in communication with the secondelectrode.
 20. A method of operating a metal oxygen battery, the methodcomprising: providing a first electrode formed of oxygen storagematerial and contains oxygen; and communicating oxygen from inside theoxygen storage material of the first electrode to outside of the firstelectrode.